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dc.contributor.author윤주영*
dc.contributor.authorYin Jun*
dc.date.accessioned2016-08-29T12:08:58Z-
dc.date.available2016-08-29T12:08:58Z-
dc.date.issued2015*
dc.identifier.issn1359-7345*
dc.identifier.otherOAK-14756*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/230501-
dc.description.abstractAn aryl-thioether substituted nitrobenzothiadiazole probe was synthesized and employed to detect cysteine and homocysteine selectively in living cells. Interestingly, both cysteine (Cys) and homocysteine (Hcy) promote an enhancement of the fluorescence intensity of the probe at pH 7.4 while only Cys gives rise to this enhancement under weakly acidic conditions (pH 6.0). This journal is © The Royal Society of Chemistry 2015.*
dc.languageEnglish*
dc.publisherRoyal Society of Chemistry*
dc.titleAn aryl-thioether substituted nitrobenzothiadiazole probe for the selective detection of cysteine and homocysteine*
dc.typeArticle*
dc.relation.issue30*
dc.relation.volume51*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage6518*
dc.relation.lastpage6520*
dc.relation.journaltitleChemical Communications*
dc.identifier.doi10.1039/c5cc01071c*
dc.identifier.wosidWOS:000352269000011*
dc.identifier.scopusid2-s2.0-84926390458*
dc.author.googleLee D.*
dc.author.googleKim G.*
dc.author.googleYin J.*
dc.author.googleYoon J.*
dc.contributor.scopusid윤주영(7403587371)*
dc.contributor.scopusidYin Jun(56438439100)*
dc.date.modifydate20240405125409*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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